Tanaka Sakae
Department of Orthopedic Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
J Orthop Sci. 2018 Sep;23(5):717-721. doi: 10.1016/j.jos.2018.06.001. Epub 2018 Jun 30.
Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder characterized by progressive destruction of affected synovial joints. Recently, it was demonstrated that osteoclasts play critical roles in bone destruction in RA. Receptor activator of NF-κB ligand (RANKL), which belongs to the tumor necrosis factor superfamily, is indispensable for osteoclast differentiation and bone destruction in RA. Denosumab, a monoclonal antibody against human RANKL, not only increased bone mineral density, but also efficiently suppressed the progression of bone erosion in RA patients in a randomized controlled study. However, denosumab did not reduce the cartilage destruction or disease activity in RA, and further investigation is required to establish the appropriate positioning of denosumab in the treatment strategy of RA.
类风湿性关节炎(RA)是一种自身免疫性炎症性疾病,其特征是受累滑膜关节进行性破坏。最近有研究表明,破骨细胞在类风湿性关节炎的骨破坏中起关键作用。核因子κB受体活化因子配体(RANKL)属于肿瘤坏死因子超家族,是类风湿性关节炎中破骨细胞分化和骨破坏所必需的。在一项随机对照研究中,抗人RANKL单克隆抗体地诺单抗不仅增加了骨密度,还有效抑制了类风湿性关节炎患者的骨侵蚀进展。然而,地诺单抗并没有减少类风湿性关节炎中的软骨破坏或疾病活动,需要进一步研究以确定地诺单抗在类风湿性关节炎治疗策略中的适当定位。